Role: Associate Document Control
Job Location: Dale City, VA
Position Type: 6-Month Contract-to-Hire
Shift: Monday to Friday 7:00 AM – 3:30 PM
**Note: Onsite Interview**
Summary
This position is key in maintaining the Quality System documentation in a regulated manufacturing environment. The selected candidate will work cross-functionally to ensure compliance with internal procedures, customer requirements, and regulatory standards, including cGMP, FDA, SQF, HACCP, and FQP guidelines.
Key Responsibilities
Create, revise, and maintain Quality System documentation using technical writing best practices (formatting, numbering, version control)
Issue batch records accurately and promptly to the Production and Packaging departments
Review completed batch records to ensure compliance with internal standards and regulatory requirements
Prepare documentation and provide support during customer audits and third-party certifications
Manage routing, review, and approval of controlled documents, deviations, and change controls
Conduct internal audits to assess compliance and document all findings and non-conformances
Track, document, and assist with the implementation and verification of CAPAs (Corrective and Preventive Actions)
Collaborate in cross-functional meetings for New Product Introductions (NPIs) and Change Control processes
Maintain updated records, specifications, and documents in coordination with Production, Packaging, R&D, and other departments
Enter and track quality data using computerized systems to ensure traceability and performance monitoring
Ensure ongoing compliance with SQF, HACCP, and FQP programs
Support adherence to FDA regulations and current Good Manufacturing Practices (cGMPs)
Participate in training and development activities to support continuous improvement
Assist in ensuring the identity, purity, strength, and quality of all manufactured dietary supplement products
Perform other related duties as assigned by the Quality Management team
Qualifications & Skills
Bachelor’s degree in Food Science or related field preferred
Strong verbal and written communication skills in English (required for business and safety purposes)
Knowledge of GMP and Quality Systems
Ability to follow Standard Operating Procedures (SOPs) and Test Methods
Attention to detail and a strong sense of accountability
Self-starter with the ability to work independently with minimal supervision
Strong interpersonal and analytical skills
Ability to build collaborative relationships with cross-functional teams